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Reinhardt Pfeiffer Syndrome: Disease Bioinformatics
Reinhardt- pfeiffer Syndrome, also known as Mesolimbic dwarfism, is an autosomal dominant genetic disorder characterized by a disproportionate short stature from birth into adulthood, often accompanied by dysplasia of the ulna and fibula. Other abnormalities that have been described are curvatures of the forearm, radial head luxation, and tibial abnormalities. Reinhardt- pfeiffer Syndrome more often affects females than it does males.
Reinhardt Pfeiffer Syndrome Bioinformatics Tool
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Reinhardt Pfeiffer Syndrome below!
For more information on how to use Laverne, please read the How to Guide
Top Research Reagents
Reinhardt Pfeiffer Syndrome has been researched against:
Reinhardt Pfeiffer Syndrome has been studied in relation to diseases such as:
Alternate NamesReinhardt Pfeiffer Syndrome is also known as Reinhardt-pfeiffer Mesomelic Dysplasia, Reinhardt-pfeiffer Mesomelic Skeletal Dysplasia.